Variant #0000268562 (NC_000003.11:g.148891521T>C, HPS3(NM_032383.3):c.*1512T>C)

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.148891521T>C
DNA change (hg38) g.149173734T>C
Published as CP(NM_000096.3):c.3182-4A>G
ISCN -
DB-ID CP_000005 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00201 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CP NM_000096.3 -?/. - c.3182-4A>G r.spl? p.?
HPS3 NM_032383.3 -?/. - c.*1512T>C r.(=) p.(=)